Evidence map›Paper›PMID 34031430›Full record

ArticleScientific reports2021

Iron supplementation regulates the progression of high fat diet induced obesity and hepatic steatosis via mitochondrial signaling pathways.

Naho Kitamura, Yoko Yokoyama, Hiroki Taoka, Utana Nagano, Shotaro Hosoda, Tanon Taworntawat, Anna Nakamura, Yoko Ogawa, Kazuo Tsubota, Mitsuhiro Watanabe

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 36 citations in OpenAlex.

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  18. Iron Homeostasis and Energy Metabolism in Obesity.Clinical nutrition research · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Naho KitamuraSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan.ORCID 0000-0001-6894-3046
Yoko YokoyamaSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan.ORCID 0000-0002-4249-004X
Hiroki TaokaSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan.
Utana NaganoSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan.
Shotaro HosodaSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan.
Tanon TaworntawatSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan.
Anna NakamuraSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan.
Yoko OgawaDepartment of Ophthalmology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Kazuo TsubotaHealth Science Laboratory, Keio Research Institute at SFC, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan. tsubota@z3.keio.jp.ORCID 0000-0002-8874-7111
Mitsuhiro WatanabeSystems Biology Program, Graduate School of Media and Governance, Keio University, 5322, Endo, Fujisawa, Kanagawa, 252-0882, Japan. mitsuhiro.keio.hsl@gmail.com.ORCID 0000-0002-4500-780X
Keio University Shonan Fujisawa · JPKeio University · JPKeio University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disruption of iron metabolism is closely related to metabolic diseases. Iron deficiency is frequently associated with obesity and hepatic steatosis. However, the effects of iron supplementation on obesity and energy metabolism remain unclear. Here we show that a high-fat diet supplemented with iron reduces body weight gain and hepatic lipid accumulation in mice. Iron supplementation was found to reduce mitochondrial morphological abnormalities and upregulate gene transcription involved in mitochondrial function and beta oxidation in the liver and skeletal muscle. In both these tissues, iron supplementation increased the expression of genes involved in heme or iron-sulfur (Fe-S) cluster synthesis. Heme and Fe-S cluster, which are iron prosthetic groups contained in electron transport chain complex subunits, are essential for mitochondrial respiration. The findings of this study demonstrated that iron regulates mitochondrial signaling pathways-gene transcription of mitochondrial component molecules synthesis and their energy metabolism. Overall, the study elucidates the molecular basis underlying the relationship between iron supplementation and obesity and hepatic steatosis progression, and the role of iron as a signaling molecule.

Indexed as

AnimalsCells, CulturedDiet, High-FatDisease ProgressionEnergy MetabolismFatty LiverGene Expression ProfilingGene Expression RegulationHepatocytesIronLipid MetabolismMaleMiceMitochondrial ProteinsObesitySequence Analysis, DNAIronMitochondrial Proteins

Identifiers

PMID34031430
PMCPMC8144192
OpenAlexW3164543044

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.